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Clinical Trial Jobs (NOW HIRING)

Clinovo

Clinical Trial Manager

Waltham, MA · On-site

The Role The Clinical Trial Manager (CTM) will be a key contributor to the successful execution of clinical trials and will play an important role in building and maintaining relationships with ...

Aerogen Pharma Limited

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...

C4-Therapeutics-Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

Clinical Trial Manager Full Time Management Watertown, MA, US 23 days ago Requisition ID: 1144 Salary Range: $138,566.00 To $153,118.00 Annually About C4 Therapeutics: C4 Therapeutics (C4T) (Nasdaq:

ICON

Clinical Trial Manager

Blue Bell, PA · On-site +1

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

C4 Therapeutics Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

Job Summary C4 Therapeutics is seeking an initiative-taking Clinical Operations professional to lead the successful execution of assigned clinical trial(s) in oncology from First in Human through ...

Icon plc

Clinical Trial Manager

Blue Bell, PA · On-site

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

VENESCO, LLC

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Description Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in ...

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How much do clinical trial jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical trial in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a clinical trial role?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies.
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Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

Waltham, MA • On-site

Clinovo
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Clinovoexternal

Contractor

Posted 12 days ago

Job description

The Role
The Clinical Trial Manager (CTM) will be a key contributor to the successful execution of clinical trials and will play an important role in building and maintaining relationships with investigators, study site personnel, CRAs, CRO teams, and external vendors.
Leveraging a strong understanding of clinical trial execution, the CTM will oversee day-to-day clinical trial operations, including clinical project management, study site activities, CRA monitoring activities, and vendor management.
The CTM will work closely with cross-functional study teams to ensure assigned clinical trials are executed according to established timelines, quality standards, budgets, and applicable regulatory requirements.
Key Responsibilities
  • Manage and lead the day-to-day operations of assigned clinical trial(s), ensuring execution against established study goals, timelines, and objectives and in compliance with applicable GCP/ICH guidelines and regulatory requirements.
  • Participate in and, depending on study scope, lead cross-functional study teams, including CROs and external vendors.
  • Coordinate with internal functional areas to ensure effective execution of clinical study activities.
  • Support laboratory-related study activities, including understanding study sampling requirements and providing oversight of laboratory vendors in collaboration with cross-functional teams.
  • Develop and/or contribute to informed consent forms (ICFs), study training materials, and study-specific tools.
  • Provide Clinical Operations input into protocols, ICFs, CRF design, monitoring conventions, edit checks, and vendor specifications.
  • Review, approve, and provide timely sign-off on key study documents.
  • Provide sponsor oversight of CROs and third-party vendors to ensure compliance with study protocols, contractual requirements, timelines, and defined scopes of work.
  • Monitor CRO and vendor performance, identify potential issues, and escalate concerns to Clinical Operations leadership when appropriate.
  • Interpret study protocols and effectively communicate protocol requirements to study teams, sites, and external partners.
  • Proactively identify study risks and develop mitigation strategies in collaboration with cross-functional stakeholders.
  • Manage study timelines, milestones, and deliverables and provide regular progress updates to management.
  • Develop and maintain study metrics and tracking tools, including patient visits, data entry, monitoring activities, data cleaning, and other key operational indicators.
  • Support study financial management activities, including review of contracts, budgets, invoices, and statements of work.
  • Contribute functional Clinical Operations expertise to the development and implementation of SOPs.
  • Partner closely with Data Management, Biostatistics, Regulatory Affairs, Pharmacovigilance, and other functions throughout study execution.
  • Support study inspection readiness and ensure appropriate documentation and processes are maintained throughout the clinical trial lifecycle.
Desired Experience & Qualifications
  • Bachelor's degree in life sciences, healthcare, or a related discipline.
  • Minimum of 5 years of clinical trial management experience within the pharmaceutical, biotechnology, or CRO industry, with progressively increasing Clinical Operations responsibilities.
  • Strong understanding of the complete clinical trial lifecycle, from study start-up through close-out.
  • Experience supporting inspection readiness activities.
  • Experience providing oversight of CROs and external service providers.
  • Experience managing or supporting international clinical trials, including studies conducted across multiple global regions.
  • Oncology clinical trial experience preferred.
  • Working knowledge of GCP, ICH guidelines, FDA regulations, and other applicable clinical research requirements.
  • Strong understanding of cross-functional clinical development disciplines, including Data Management, Biostatistics, Regulatory Affairs, and Pharmacovigilance.
  • Demonstrated ability to lead effective study team meetings and facilitate cross-functional decision-making.
  • Strong judgment with the ability to proactively identify, communicate, and resolve study-related risks and issues.
  • Excellent verbal and written communication skills with the ability to effectively interact with internal and external stakeholders.
  • Strong organizational and prioritization skills with the ability to work independently and manage multiple priorities.
  • Ability to travel approximately 5-10%, including domestic and international travel.

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